Anfíbios Anuros da coleção Adolpho Lutz: III - Hyla claresignata Lutz & B. Lutz, 1939

Hyla claresignata Lutz & Lutz, 1939, is a large species apparently not closely allied to the other known Brazilian hylas. It is characterized by the very small tympanum; the head is short and the snout rounded; the legs are long, the hands and feet unusually large, the latter extensively webbbed. The specific name is derived from the insular, irregular, or roughly triangular, dark spots, with a light halo, found mostly in the dorso-lateral region and on the legs. It belongs to the rain-forest fauna of the Marítime Range. The adult is a bromeliad-dweller and the tadpole rhyacophilous. DESCRIPTION. Vomerine teeth in two separate, oblique, groups, behind the large choanae, parallel to the posterior half of their inner border. Tongue entire, short, very broad and hardly free behind. Snout short, rounded, with distinct canthus rostralis and gradually sloping loreal region. Eye very large and prominent, its horizontal diameter almost equal to the distance between its anterior corner and the tip of the snout. Tympanum very small, less than one third of the diameter of the eye, but distinct, partly covered by a short, heavy ridge. Lateral fingers less than one third webbed; fourth finger slightly longer than the second, just reaching the base of the disk of the third; subarticular tubercles well developed; an angular pollex rudiment, more noticeable in the males. Toes almost completely webbed, the edge of the web inserted at the base of the disk on the third and the fifth; an inner metatarsal tubercle. Skin smooth above, granular beneath, on the throat minutely so. No dermal appendage on the hell. Habit robust, head broader than long, body rather heavy, slightly narrowed in the postaxillary region. Legs long, the tibiotarsal articulation reaching beyond the tip of the snout when adpressed. Type (female): 61 mm. (Fig. 1.) DIAGNOSIS of TADPOLE (by G. Orton). "A large specialized, mountain-stream tadpole, with wide head an elongated, flattened snout, greatly enlarged lips and high tooth formula. Eyes dorsal. Spiracle sinistral, projecting, situated far back on side. Anus dextral. Tooth formula 8/12 to 9/14 in fully grown larvae. Tail with a prominent, vertical dark band across musculature and fins; a second concentration of dark pigment near tip of tail, may or may not form a similar but narrower band. Maximum known total length: 60mm.; head and body length 25mm. (Figs. 6 e 7). For further details see Lutz & Lutz, 1939 and Lutz B. & Orton G. 1946.

Notas de ixodologia: V - A propósito da validade de algumas espécies do gênero Amblyomma do continente americano (Acari: Ixodídoe)

a) The species Amblyomma tapiri Tonelli Rondelli, 1937 and Amblyomma finitimum Tonelli Rondelli, 1937 are synonymous with Amblyomma cajennense Fabricius, 1787. Both species are based in differences of size, colour, punctations and form of the dorsal shield, presence or absence of ventral plates, size, form and direction of the spine of coxa IV. Such differences prouved to be only variations frequently observed in large lots or in cultures of Amblyomma cajennense. The revalidation of Koch's species Amblyomma tenellum Koch, 1844 and Amblyomma mixtum Koch, 1844 proposed by TONELLI RONDELLI as also of Amblyomma sculptum Berlese, 1888 and Amblyomma versicolor Nuttal et Warburton, 1908 cannot be accepted by the same reasons. b) Amblyomma beccari Tonelli Rondelli, 1939 and Amblyomma latepunctatum Tonelli Rondelli, 1939 are cospecific with Amblyomma scalpturatum Neumann, 1899 the same being true for Amblyomma myrmecophagium Schulze, 1935 and for Amblyomma brasiliense var. guianense Floch et Abonnenc, 1940, as previously stated. c) Amblyomma tasquei Floch et Abonnenc, 1940 is a good species but synonym with Amblyomma romitii Tonelli Rondelli, 1939 which has priority. d) Amblyomma curruca Schulze, 1936 is a synonym of Amblyomma parvum Aragão, 1908. e) Amblyomma deminutivum Neumann, 1899 represents a variation of Amblyomma dissimile Koch, 1844, a species whose internal spine of coxa IV may be poorly developed or even absent. f) Amblyomma nigrum Tonelli Rondelli, 1939 prouved to be synonym with Amblyomma paccae Aragao, 1911 the type representing a blackish specimen of the later species. g) Amblyomma brimonti Neumann, 1913 is a synonym of Amblyomma humerale Koch, 1844.

Nota sobre Lutzomyia (Trichopygomyia) Dasypodogeton (Castro, 1939), com a redescrição do macho e da fêmea (Diptera: Psychodidae, Phlebotominae)

Os autores, após transcreverem a descrição original da Lutzomyia (Trichopygomyia) dasypodogeton (Castro, 1939), inicialmente publicada de maneira muito resumida em jornal não científico, redescrevem, de acordo com as normas atualmente adotadas, ambos os sexos dessa espécie, inclusive com desenhos dos elementos taxonomicamente importantes. É, também, dada uma chave para a identificação das espécies do subgênero trichopygomyia Barreto, 1952.

Report of Lepocreadium Bimarium manter, 1940, Vitellibaculum Spinosa (Siddioi) & Cable, 1960) and Hirudinella Ventricosa (Pallas, 1774), parasites of marine fishes in Brazil

Lepocreadium bimarinum and Vitellibaculum spinosa are referred for the first time in Stephanolepis hispidus and in Brazil, and Hirudinella ventricosa is reported from Scomberomorus cavalla. Measurements, figures and comments are given.

Some new species of Caryospora (Apicomplexa: Eimeriidae) from brazilian snakes, and a re-description of C. jararacae Carini, 1939

The mature ooxysts of six new species of Caryospora are described from the faeces of Brazilian snakes. They are differentiated from other species previously recorded from reptiles, largely on the size and shape of the oocyst and sporocyst, structure of the oocyst wall, and presence or absence of a polar body. C. paraensis n. sp., and C. carajasensis n. sp., are from the "false coral", Oxyrhopus petola digitalis; C. pseustesi n. sp., from the "egg-eater", Pseustes sulphureus sulphureus; C. epicratesi n. sp., from the "red boa", Epicrates cenchria cenchria; and C. micruri n. sp., and C. constancieae n. sp., from the "coral snake", Micrurus spixii spixii. A re-description is given of C. jararacae Carini, 1939, from the "jararaca" Bothrops atrox, embodying some additional morphological features.

Estudo comparativo da genitália externa masculina de Triatoma neotomae Neiva, 1911 e Triatoma nitida Usinger, 1939 (Hemiptera, Reduviidae)

The morphological comparative study of the phallus organs, of both species, shown five structures wich may be used as taxonomic characters. They are: parameres (Pa), median process pygophore (PrP), basal plate (EPbi), gonopore (PrG) and endosoma process (PrEn).

Biologia do Triatoma nitida Usinger, 1939 em laboratório (Hemiptera: Reduviidae)

Triatoma nitida is a wild species occurring in Mexico and Central America. In order to establish the length of its life cycle and transmission potential, the following parameters were observed: the incubation period, the interval between hatching, or moulting, and the first feeding; the number of blood meals and the time of development. The time-lapse before the bite, the length of feeding and the interval between the end of the blood meal and defecation, as well as the site of defecation were also analyzed. Average length of the egg incubation period was 18.2 days. Time interval between the food source offering and the bite was less than 4 min in 60//of the analyzed cases, except in the fifth instar, where only 38//of the insects began feeding in less than 5 min. The blood-sucking period was long and rising until the fifth instar, decreasing in adults, and ranging from 1 min to 2 and a half hours. Only 26//of the blood meals were followed by defecations within 20 min. The average length of the life cycle was 897.5 days.

Variation between geographical populations of Lutzomyia (Nyssomyia) whitmani (Antunes & Coutinho, 1939) sensu lato (Diptera:Psychodidae:Phlebotominae) in Brazil

Phylogenetic analysis of morphometric and biological characters indicated that there are two distinct forms of Lutzomyia whitmani in Brazil: one is present both north and south of the River Amazonas in the State of Pará while the other occurs in northeast Brazil, in the State of Ceará, and further south, including the type locality in State of Bahia. The Amazonian form is reportedly neither strongly anthropophilic nor synanthropic, and it is the vector of Leishmania shawi; whereas the southern form is often collected peridomestically, while biting man, and has been found infected with Le.(V.) braziliensis. The ratio of the length of the genital filaments to that the genital pump was found to be consistently smaller in males of the Amazonian populations. A middle repetitive DNA element was isolated by differentially screening a genomic library made using Amazonian material, and the sequence was diagnostic for this form of Lu. whitmani (being absent or occurring in low copy number in the southern form). The total evidence suggests there are at least two, geographically-isolated forms of Lu. whitmani, which may represent different cryptic species.

Distribuição Geográfica e Dispersão Alti-latitudinal de Alguns Gêneros e Espécies da Tribo Triatomini Jeannel, 1919 (Hemiptera, Reduviidae, Triatominae)

Geographical Distribution and Alti-latitudinal Dispersion of Some Genera and Species of the Tribe Triatomini Jeannel, 1919 (Hemiptera, Reduviidae, Triatominae) - With the currently known distribution of genera and species of the tribe Triatomini Jeannel, 1919, maps and diagrams were prepared, showing the geographical area occupied by the species and their respective dispersion in grades of latitude and altitude. Two genera are not treated: Panstrongylus Berg, 1879, already published and Triatoma Laporte, 1832, that is being published partially in several articles. Genus Eratyrus Stal, 1859, has two species, while Dipetalogaster Usinger, 1939, Mepraia Mazza, Gajardo & Joerg, 1940, Paratriatoma Barber, 1938 and recently created genus Hermanlentia Jurberg & Galvão, 1997, have only one each. The study of these maps and diagrams permits a better knowledge about some ecological requirements of Chagas' disease vectors and detects gaps in the geographical distribution, where the species were not found but probably they could be prevalent

Gregarine Cephaloidophora communis mawrodiadi, 1908 in the barnacle Euraphia rhyzophorae, Oliveira, 1940 from Brazil

The gregarine Cephaloidophora communis was observed for the first time in Brazil in the barnacles Euraphia rhyzophorae collected in Angra dos Reis, Rio de Janeiro, Brazil, between 1990 and 1996. Histological studies showed growth phases of the parasite in specific parts of the digestive system. The intracellular forms occurred in the vacuoles of the intestinal cells. Syzygy was frequent, and the most common form following syzygy was cylindrical, with a single membrane. The cytoplasm of the gregarines was always irregular, dense, and occasionally presenting a dark stoch area.

Geographic distribution and morphometric differentiation of Triatoma nitida usinger 1939 (Hemiptera: Reduviidae: Triatominae) in Guatemala

Triatoma nitida was found in 14 (0.4%) out of 3,726 houses located in six departments across Guatemala, which were surveyed from 1994 to 1998 by the man-hour collection method. Compared to previous information, the distribution of T. nitida in Guatemala has increased from five to nine departments; the species is present in mild climates at altitudes from 960 to 1,500 m. Fourteen percent of the intradomestic T. nitida were infected with Trypanosoma cruzi. The species was often found in conjunction with other triatomines (T. dimidiata and Rhodnius prolixus). The domestic and peridomestic presence of T. nitida in Guatemala was rare, but occasionally this species was colonizing human-made constructions. T. nitida appears to have a low importance as Chagas disease vector in Guatemala, as indicated by its scarce presence in the domestic habitats and defecation patterns. However, it clearly has potential to become a Chagas vector so we recommend an on-going study of the intradomestic presence of T. nitida following the control programs in Guatemala. Morphometric analysis of 47 T. nitida males from three localities showed quantitative differences between the populations, which indicates that geographic distance is an important factor in the structuring of T. nitida populations.